HomeUSAAsia Dynamics, Inc.

Asia Dynamics, Inc.

USA · Chicago
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
23listed device types
Class I 20Class II 2Class III 0unclassified 1
plus 23 registration records and 5 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
3 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States23 registration records, 5 510(k), 0 PMA, 65 excluded
Brazil0 confirmed, 9 excluded
Canada0 confirmed, 9 excluded
Manufacturer names merged into this page: JINGMEN HUASHENG ASIA DYNAMICS SANITARY PRODUCTS CO., LTD. · ASIA DYNAMICS INC. DBA ADI MEDICAL

Company information

Country
USA
City
Chicago

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

11989 · K891160
21995 · K953501
11996 · K953500
12022 · K213347

FDA listed device types

showing 8 of 23
Cap, Surgical 1Forceps 1Clamp 1Bedding, Disposable, Medical 1Tape And Bandage, Adhesive 1Tourniquet, Nonpneumatic 1Sling, Arm 1Device, Fixation, Tracheal Tube 1

Registration details (sample)

MarketIdentifierNameClass / date
USK213347ADI Medical Surgical Face Mask2022-01-25
USK953500HEMO-BARRIER1996-01-24
USK953501ADI STERILE GAUZE SPONGES1995-08-28

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